Found: 6
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Fetal and neonatal outcomes of posterior fossa anomalies: a retrospective cohort study.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-59163-8
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- Publication type:
- Article
The rate of secondary genomic findings in the Saudi population.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 1, p. 83, doi. 10.1002/ajmg.a.62491
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- Publication type:
- Article
Genomic testing and counseling: The contribution of next‐generation sequencing to epilepsy genetics.
- Published in:
- Annals of Human Genetics, 2020, v. 84, n. 6, p. 431, doi. 10.1111/ahg.12397
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- Publication type:
- Article
A mendelian form of neural tube defect caused by a de novo null variant in SMARCC1 in an identical twin.
- Published in:
- 2018
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- Publication type:
- journal article
Blepharo-cheilo-dontic (BCD) syndrome: Expanding the phenotype, case report and review of literature.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 6, p. 1525, doi. 10.1002/ajmg.a.36465
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- Publication type:
- Article
Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 12, p. 3155, doi. 10.1002/ajmg.a.36160
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- Publication type:
- Article